Mapping Amyloid Networks in Alzheimer's Disease: A High-Order ICA Approach to Gray and White Matter Pathology
Nigar KhasayevaiD, Kyle M. JenseniD, Cyrus EierudiD, Helen Petropoulos, Allan I. LeveyiD, James J. LahiD, Ruiyan LuoiD, Enrico PremiiD, Barbara BorroniiD, Jiayu CheniD, Vince D. CalhouniD, Armin IrajiiD
Abstract
INTRODUCTIONAlzheimers Disease (AD) is a neurodegenerative disorder marked by gray matter (GM) changes driven by amyloid-beta (A{beta}) plaques and neurofibrillary tangles. While GM alterations are well documented, spatially distinct patterns of homogeneous A{beta} uptake and white matter (WM) involvement remain underexplored. METHODSWe applied high-order independent component analysis (ICA) to 716 [18F]Florbetapir PET scans, identifying 80 GM and 13 WM networks. Diagnostic and cognitive associations were evaluated via statistical modeling. RESULTSIdentified networks delineated a progression trajectory, with mild cognitive impairment (MCI) profiles in temporoparietal and frontal subdomains more closely aligned with AD than cognitively normal (CN) profiles. GM networks, including the hippocampal-entorhinal complex and precuneus, and WM networks, including the retrolenticular internal capsule, demonstrated robust associations with cognitive performance. DISCUSSIONOur findings highlight the utility of high-order ICA in identifying reproducible A{beta} networks and the contribution of WM networks, such as the posterior corpus callosum, in the early pathological landscape of AD.
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